Tert-Butyl 3-amino-5-fluoropiperidine-1-carboxylate is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. This compound features a tert-butyl ester group, contributing to its lipophilicity and stability. The presence of an amino group at the 3-position and a fluorine atom at the 5-position of the piperidine ring enhances its potential for biological activity, making it of interest in medicinal chemistry. The carboxylate functional group is typically involved in various chemical reactions, including esterification and amidation. This compound may exhibit specific solubility properties in organic solvents and water, influenced by the tert-butyl group and the polar amino and carboxylate functionalities. Its molecular structure suggests potential applications in drug development, particularly in the design of compounds targeting specific biological pathways. As with many fluorinated compounds, it may also exhibit unique pharmacokinetic properties, such as altered metabolic stability. Overall, tert-Butyl 3-amino-5-fluoropiperidine-1-carboxylate represents a versatile scaffold for further chemical modifications and investigations.

tert-Butyl 3-amino-5-fluoropiperidine-1-carboxylate

1356342-41-0: Tert-Butyl 3-amino-5-fluoropiperidine-1-carboxylate is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. This compound features a tert-butyl ester group, contributing to its lipophilicity and stability. The presence of an amino group at the 3-position and a fluorine atom at the 5-position of the piperidine ring enhances its potential for biological activity, making it of interest in medicinal chemistry. The carboxylate functional group is typically involved in various chemical reactions, including esterification and amidation. This compound may exhibit specific solubility properties in organic solvents and water, influenced by the tert-butyl group and the polar amino and carboxylate functionalities. Its molecular structure suggests potential applications in drug development, particularly in the design of compounds targeting specific biological pathways. As with many fluorinated compounds, it may also exhibit unique pharmacokinetic properties, such as altered metabolic stability. Overall, tert-Butyl 3-amino-5-fluoropiperidine-1-carboxylate represents a versatile scaffold for further chemical modifications and investigations.

CAS 1356342-41-0

tert-Butyl 3-amino-5-fluoropiperidine-1-carboxylate

tert-Butyl 3-amino-5-fluoropiperidine-1-carboxylate

Ref: IN-DA01B2RM

tert-Butyl 3-amino-5-fluoropiperidine-1-carboxylate

Ref: 10-F693568